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MW 289.4 Da, Purity >98%. Potent, competitive, non-selective mAChR antagonist (IC50 = 2.5 nM). Induces mydriasis. Shows antimuscarinic and anticholinergic effects in vivo. Orally active.

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Images

Chemical Structure - Atropine, mAChR antagonist (AB145582), expandable thumbnail

Publications

  • The Journal of neuroscience : the official journal of the Society for Neuroscience 43:722-7352022
    Differential Regulation of Prelimbic and Thalamic Transmission to the Basolateral Amygdala by Acetylcholine Receptors.
    Applications:
    Unspecified application
    Reactive species:
    Unspecified reactive species
    Sarah C Tryon,Joshua X Bratsch-Prince,James W Warren,Grace C Jones,Alexander J McDonald,David D Mott
    PubMed 36535767
  • The Journal of surgical research 244:358-3672019
    M1 Macrophage Activated by Notch Signal Pathway Contributed to Ventilator-Induced Lung Injury in Chronic Obstructive Pulmonary Disease Model.
    Applications:
    Unspecified application
    Reactive species:
    Unspecified reactive species
    Hongping Huang et. al.
    PubMed 31323391

Key facts

CAS number

51-55-8

Purity

> 98%

Form

Solid

Source

Solanaceae sp.

Molecular weight

289.4 Da

Molecular formula

C17H23NO3

PubChem identifier

3661

Nature

Native

Alternative names

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MW 289.4 Da, Purity >98%. Potent, competitive, non-selective mAChR antagonist (IC50 = 2.5 nM). Induces mydriasis. Shows antimuscarinic and anticholinergic effects in vivo. Orally active.

Alternative names

Key facts

Purity

> 98%

Source

Solanaceae sp.

PubChem identifier

3661

Solubility

Crystals, mp 222-223 °C. Sol in 1 part water; slightly sol in alc. Almost insol in chloroformm ether. /Methylbromide/. Crystals, mp 163 °C. Freely sol in water or alc, very slightly in chloroform, ether. /Methylnitrate/. Crystalline powder, mp 127-128 °C, dec 135 °C. Very hygroscopic. Soluble in alc, chloroform. Practically insol in ether, /N-oxide/. 1 g in: ... 2 mL alcohol, 25 mL ether, 27 mL glycerol, 1 mL chloroform; also sol in benzene, in dil acids. Very soluble in ethanol; slightly soluble in chloroform; insoluble in ethyl ether. In water, 2,200 mg/l @ 25 °C.

Biochemical name

L-Hyoscyamine

Biological description

Potent, competitive, non-selective mAChR antagonist (IC50 = 2.5 nM). Induces mydriasis. Shows antimuscarinic and anticholinergic effects in vivo. Orally active.

Canonical SMILES

CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3

InChI

InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3

InChIKey

RKUNBYITZUJHSG-UHFFFAOYSA-N

IUPAC name

(8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 3-hydroxy-2-phenylpropanoate

Storage

Shipped at conditions

Ambient - Can Ship with Ice

Appropriate short-term storage conditions

Ambient

Appropriate long-term storage conditions

Ambient

Storage information

The product can be stored for up to 12 months

Supplementary info

Activity summary

Muscarinic Acetylcholine Receptor M3 also known as CHRM3 or M3 receptor plays an important role in various physiological processes. This receptor is part of the G-protein coupled receptor family and binds acetylcholine. The mass of CHRM3 is around 65 kDa. CHRM3 is widely expressed in various tissues including smooth muscle exocrine glands and in some cases the central nervous system. This extensive expression indicates its significance in multiple bodily functions.

Biological function summary

CHRM3 mediates cellular responses such as smooth muscle contraction and glandular secretion. It operates as part of a larger receptor complex that facilitates the signal transduction process. When acetylcholine binds to CHRM3 it activates downstream signaling pathways involving various intracellular messengers. This activation influences activities such as bronchoconstriction and salivation emphasizing the importance of M3 receptor in autonomic nervous system regulation.

Pathways

Studies show that CHRM3 engages with the inositol phospholipid-calcium signaling pathway. This pathway mobilizes calcium from intracellular stores working together with proteins like G-proteins and protein kinase C. These interactions lead to physiological effects such as muscle contraction and secretion. Moreover CHRM3 links with the MAPK/ERK pathway conveying signals that influence cell growth and differentiation. The intertwining of these pathways highlights CHRM3’s role in regulating key cellular functions.

Associated diseases and disorders

CHRM3’s malfunction associates with asthma and chronic obstructive pulmonary disease (COPD). Dysregulated CHRM3 signaling can exacerbate symptoms involving bronchoconstriction and mucus secretion. Furthermore CHRM3 connects to proteins affecting airway smooth muscle cells intensifying disease conditions. Its relevance in exocrine gland regulation also implicates CHRM3 in conditions like Sjögren's syndrome where it may impact salivary and lacrimal gland secretion. Understanding these connections aids in developing targeted therapies for these ailments.

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1 product image

  • Chemical Structure - Atropine, mAChR antagonist (ab145582), expandable thumbnail

    Chemical Structure - Atropine, mAChR antagonist (ab145582)

    2D chemical structure image of ab145582, Atropine, mAChR antagonist

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Product protocols

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